Remco Munnik, our Regulatory Information Director, attended the European Union International Organization for Standardization (ISO) identification of medicinal products (IDMP) Task Force meeting.
The meeting between representatives from the European Medicines Agency, terminology organisations, software vendors and developers of medicinal product dictionaries/databases was held to discuss aspects of planning, development, implementation and maintenance of the ISO IDMP standards in the EU, in line with requirements defined at international level and based on agreed EU implementation principles.
For more information on the meeting and the presentations, please check this link.
If you have any doubts regarding ISO IDMP implementation, please do not hesitate to contact us at [email protected]
